Canonical Allele Identifier: CA2718433768
Gene:

Linked Data

dbSNP Id: rs921797568

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.1787506A>T , CM000671.2:g.1787506A>T GRCh38
NC_000009.11:g.1787506A>T , CM000671.1:g.1787506A>T GRCh37
NC_000009.10:g.1777506A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746599.1:n.142+68594A>T